Classified by application
All Products
Signaling Pathways
- Angiogenesis/Protein Tyrosine Kinase
- Apoptosis Pathway
- Cell Cycle/DNA Damage
- Epigenetics
-
GPCR/G Protein
- Melatonin Receptor
- Urotensin Receptor
- Neurotensin Receptor
- Motilin Receptor
- Glucose Transporter
- Adenylate Cyclase
- Cholecystokinin Receptor
- TGR5
- Bradykinin Receptor
- Oxytocin Receptor
- Somatostatin Receptor
- Guanylate Cyclase
- Melanocortin Receptor
- Imidazoline Receptor
- Neuropeptide Receptor
- PAR
- CRFR
- Sigma Receptor
- S1P Receptor
- GHSR
- PKA
- OX Receptor
- Adenosine Receptor
- Glucagon Receptor
- Prostaglandin Receptor
- NK Receptor
- GnRH Receptor
- Leukotriene Receptor
- Glucocorticoid Receptor
- mAChR
- P2 Receptor
- GPR
- CGRP Receptor
- CXCR
- Histamine Receptor
- CaSR
- Ras/Rho
- Vasopressin Receptor
- Smoothened/Smo
- Opioid Receptor
- mGluR
- Cannabinoid Receptor
- Dopamine Receptor
- Angiotensin Receptor
- Adrenergic Receptor
- SGLT
- Endothelin Receptor
- CCR
- 5 HT Receptor/Serotonin Receptor
- Hormone Pathay
- Ion Channel/Membrane Transporter
- Jak/Stat Pathway
- MAPK Pathway
- Microbiology/Virology
-
Neuro Signaling Pathway
- Imidazoline Receptor
- Monoamine Oxidase
- COMT
- Amyloid β
- NK Receptor
- Beta secretase
- AChE
- SSRI
- CaMK
- P glycoprotein
- Opioid Receptor
- Dopamine Receptor
- Adrenergic Receptor
- mGluR
- Histamine Receptor
- Gamma secretase
- Dopamine Transporter
- 5 HT Receptor/Serotonin Receptor
- FAAH
- P2 Receptor
- nAChR
- CGRP Receptor
- COX
- GABA Receptor
- mAChR
- NFκB
- PI3K/Akt/mTOR
-
Protease/Metabolic Enzyme
- 11β HSD
- COMT
- Carboxypeptidase
- ACC
- Xanthine Oxidase
- Mitochondrial Metabolism
- Pyruvate Kinase
- SCD
- ALDH
- Serine Protease
- Neprilysin
- CETP
- FTase
- MLR
- MAGL
- Carbonic Anhydrase
- E1 E2 E3 Enzyme
- Elastase
- Glucokinase
- ROR
- NOX
- PAI1
- Aldose Reductase
- Tyrosinase
- FAS
- DGAT
- Lipoxygenase
- Nampt
- IDO
- IDH
- MMP
- Cathepsin
- Phosphatase
- Thrombin
- FXR
- RAR/RXR
- HMGCR
- FAAH
- Gamma secretase
- RAAS/ACE
- Caspase
- HIV Protease
- Aminopeptidase
- HCV Protease
- HSP
- Tryptophan Hydroxylase/TPH
- Factor Xa
- DPP
- Procollagen C Proteinase
- Integrase
- Phosphodiesterase/PDE
- Phospholipase
- LXR
- Proteasome
- Cytochrome P450
- TGF beta/Smad
- Wnt/Stem Cell
- Others Pathway
Research Areas
- Metabolic Disease
- Neurological Disease
- Endocrinology
- Diabetes
- Cardiovascular Disease
- Immunology
- Allergy
- Inflammation
- Infection
- Cancer
Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Nucleoside Series
- Azaindazole
- Pyridazine Series
- Quinazoline
- Pyrimidine Series
- Pyrazole Series
- Quinoline Series
- Boric acid
- Pyrrole Series
- Thiophene Series
- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Pyridine Series
- Benzene Series
Raw Materials
p38 MAPK
Chemical Structure | Cat. No. | Product Name | CAS No. |
---|
|
BCP37429 | AZD7624 New | 1095004-78-6 |
AZD7624 is an inhaled p38 inhibitor, with potent anti-inflammatory activity.
|
![]() |
BCP34874 | MW-150 New | 1628502-91-9 |
MW-150 is a novel potent, selective, CNS penetrant and orally active inhibitor of p38α MAPK with Ki of 101 nM
|
![]() |
BCP29070 | SB 203580 hydrochloride New | 869185-85-3 |
SB 203580 hydrochloride is a widely used p38 MAPK inhibitor. SB 203580 hydrochloride (RWJ 64809 hydrochloride) inhibits SAPK2a/p38 and SAPK2b/p38β2, with IC50s of 50 nM and 500 nM, respectively. LCK, GSK3β and PKBα are also inhibited by SB 203580 hydrochloride, but the IC50s are 100-500-fold higher than that for SAPK2a/p38.
|
![]() |
BCP27665 | LY2322600 New | 862505-01-9 |
LY2228820 is a novel and potent p38MAPK inhibitor.
|
![]() |
BCP30837 | MW-150 dihydrochloride dihydrate New | 1661020-92-3 |
MW-150 dihydrochloride dihydrate is a selective inhibitor of p38αMAPK isoform with a Ki of 101 nM.
|
![]() |
BCP30784 | ITX-5061 HCl New | 1252679-52-9 |
ITX5061 is a type II inhibitor of p38 MAPK and also an antagonist of scavenger receptor B1 (SR-B1).
|
![]() |
BCP28410 | Pexmetinib New | 945614-12-0 |
Pexmetinib is a potent Tie-2 and p38 MAPK dual inhibitor, with IC50s of 1 nM, 35 nM and 26 nM for Tie-2, p38α and p38β, respectively, and can be used in the research of acute myeloid leukemia.
|
![]() |
BCP21625 | SD-06 | 271576-80-8 |
SD-06 is a MAPK p38 alpha inhibitor for the treatment of arthritis.
|
![]() |
BCP21617 | SB202190 HCl | 350228-36-3 |
SB 202190 inhibits p38 and p38β2 with IC50 values of 50 nM and 100 nM. respectively.
|
![]() |
BCP29574 | R1487 | 449811-92-1 |
R1487 is a p38 MAP kinase inhibitor with an IC50 of 10nM.
|
